• Merck & Co. (Durham, NC)
    support VMF, including periodic shop floor audits, direct in-line Quality support for all compliance and environmental monitoring matters, review of atypical ... Floor Quality Assurance Associate role will be responsible for activities that support Good Manufacturing Practice and regulatory compliance during product… more
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  • Merck & Co. (Rahway, NJ)
    data and processes are maintained;Provide classification expertise to support trade compliance audits;Assist the development and maintenance of ... centralized trade compliance activities, GTC manages and monitors compliance with Our Company's classification standards.The Classification Specialist more
    HireLifeScience (07/03/24)
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  • Merck & Co. (Rahway, NJ)
    …requirements for a variety of reasons, from regular business data changes to compliance updates. We also develop and support custom data applications on ... Provides expertise on data migration execution or improvement in DSP Data Platform to support migration projects.Participate data migration strategy… more
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  • Merck & Co. (Rahway, NJ)
    …AI/ML products. You will be working with a scrum team comprising of data scientists, business analysts, data engineers, and subject matter experts to ... have to take a model prototype built by a data scientist and work with the team to put...the customer/stakeholder's business needs/priorities and help build solutions that support our business goals.Has overview of the DS market… more
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  • BioAgilytix (Boston, MA)
    …here at BioAgilytix.Essential ResponsibilitiesPerform Quality Control (QC) technical, scientific, and compliance review of data and documentation generated by ... need them.Our clients trust us to deliver excellence in data and bioanalysis and in this role and you...the Bioanalytical Operations group in support of regulated studies (eg GLP, GMP).Identify deviations, OOS… more
    HireLifeScience (07/01/24)
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  • Merck & Co. (Rahway, NJ)
    …role may support facility operations, process development activities, support compliance investigations/change management, author GMP documentation and ... of our enabling facilities.Additional Supported Areas: As required and in addition to support of current capital projects the Senior Specialist may provide… more
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  • Lovelace Biomedical Research Institute (Albuquerque, NM)
    …to the Contracts Manager and under general direction, the Senior Contracts Specialist will provide technical and administrative contracts support to scientific ... staff in support of the Institute's mission.The Senior Contracts Specialist will provide end-to-end execution of Federal and commercial contracts by ensuring… more
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  • Merck & Co. (Rahway, NJ)
    …in any of our enabling facilities.Additional Supported AreasAs required and in addition to support of current capital projects the Specialist may provide direct ... that provides both technical and project management responsibility. The Specialist - Manufacturing Automation position will report to the...Basis of Design Phase and will go on to support new and/or existing facilities across the Small Molecule… more
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  • Merck & Co. (North Wales, PA)
    Job DescriptionUnder the supervision of the Business Unit Finance Director, the Senior Specialist will support the goals of US Commercial team and growth of our ... Company's Human Health business. The Senior Specialist will develop a deep understanding of their business area and participate in forecasting, budgeting, and… more
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …to MM, SD, FI, etc., particularly within the biotech industry. As the functional GMS Data Specialist , you will play a vital role in executing and overseeing the ... of multiple myeloma. Legend Biotech is seeking a Master Data Governance Sr. Specialist as part of...guides, to ensure a comprehensive knowledge base. Manage and support all site-specific projects with respect to new product… more
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  • Merck & Co. (North Wales, PA)
    …the Company Product Literature Database to ensure the maximum performance, reliability, data integrity, security, copyright compliance , and precision and recall ... Job DescriptionPosition Description: Senior Specialist , Clinical Literature MonitoringProvides pertinent and timely information on our Company's products and… more
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  • Merck & Co. (Rahway, NJ)
    … - Manufacturing Automation include the following:Site Operations (GWES) :- The Automation specialist will help to support several automation systems across the ... parts of the system as needed.Additional Supported AreasAs required and in addition to support of current capital projects the Specialist may provide direct … more
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  • Catalent (Manassas, VA)
    POSITION SUMMARYThe Quality Assurance Specialist I is responsible for inspection and verification of the products and production processes along all the production ... Report any housekeeping issues that need attention. Document all areas of non- compliance and ensure corrective actions are completed. Utilize computer to enter and… more
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  • Merck & Co. (Rahway, NJ)
    …audit activities.Ensure effective follow-up audits of sites with significant quality and compliance issues. Support the conduct effective "For Cause" audits to ... are necessary due to audit findings.Assure maintenance of audit data in a related data system (incl....of emerging regulatory and PV trends to help avoid compliance risks.Provide effective support during regulatory inspections… more
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  • Merck & Co. (North Wales, PA)
    …the chance to collaborate with our Veterans Leadership Network and receive support from various stakeholders within the organization. To ensure your success, each ... access to a career development advisor who will offer support and guidance in managing your career. - As...sensitivity, and impact which is critical to maintaining regulatory compliance . This team also monitors a list of relevant… more
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …Specifications (URS) and oversee the management of equipment qualifications. Provide support for data integrity assessments within the laboratory. Take ... treatment of multiple myeloma. Legend Biotech is seeking QC Specialist , Equipment Management as part of the Quality team...of system audit trails / periodic review to ensure data integrity and compliance . Manage equipment access… more
    HireLifeScience (06/18/24)
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  • Insmed Incorporated (Phoenix, AZ)
    …of trust, respect, and commitment to winning the right way (culture of compliance ). Foster an entrepreneurial spirit with a focus on ownership and accountability to ... and leadership. Collaborate with cross functional partners (Market Access, Patient Support ) to achieve shared business objectives in a compliant manner. Identify… more
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  • Eisai, Inc (Nutley, NJ)
    …mild cognitive impairment due to Alzheimer's disease (AD) or mild AD. TheNeurology Account Specialist (NAS) will be part of a diverse team of sales professionals who ... support this important launch and will be responsible for...cross-functionally while adhering to all of Eisai's ethics and compliance standards. Essential Functions Develop and maintain superior clinical… more
    HireLifeScience (06/14/24)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …in the treatment of multiple myeloma. Legend Biotech is seeking a CQV Specialist (Contract Position) as part of the Technical Operations team based in Raritan, ... position will be responsible for providing Commissioning, Qualification and Validation support to the cGMP Clinical and Commercial Cell Therapy Manufacturing plant.… more
    HireLifeScience (05/30/24)
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  • Novo Nordisk Inc. (West Lebanon, IN)
    …Position This position is responsible for performing reviews of manufacturing and support documentation and records to certify compliance with in-house ... assesses deviations; includes tracking, follow-up and reporting/trending Reviews manufacturing and support records to certify compliance with specifications and… more
    HireLifeScience (05/25/24)
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